Canonical Allele Identifier: PA658670507
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 477327
ClinVar RCV Id: RCV000549713 RCV001013214 RCV001107245 RCV001107247 RCV001107244 RCV001107246 RCV002491103
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Arg600Trp
CA035694
NM_020975.6:c.1798C>T